Researcher
Koenraad Devriendt
- Disciplines:Genetics, Systems biology, Medical imaging and therapy, Molecular and cell biology, Other paramedical sciences
Affiliations
- Laboratory for Genetics of Human Development (Division)
Responsible
From1 Jan 2008 → Today - Department of Human Genetics (Department)
Member
From1 Oct 1999 → Today
Projects
1 - 10 of 21
- Training teams to decipher developmental disorders in AfricaFrom1 Sep 2023 → TodayFunding: VLIR-UOS International Training Program (ITP)
- DECIPHERING DEVELOPMENTAL DISORDERS IN CENTRAL AFRICAFrom18 Feb 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- A network for research and multidisciplinary medical care for oculocutaneous albinism in the DR CongoFrom1 Jan 2020 → 31 Aug 2022Funding: VLIR-UOS South Initiatives
- IMPLEMENTATION OF GENOME-WIDE CELL-FREE DNA SEQUENCING FOR THE EARLY IDENTIFICATION AND EFFICIENT MANAGEMENT OF HIGH-RISK PREGNANCIESFrom1 Nov 2019 → 10 Oct 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- Deep familial phenotyping and genotyping to resolve phenotypic variability of inherited pathogenic genetic variantsFrom1 Oct 2019 → 30 Sep 2023Funding: BOF - projects
- Long Read Sequencing for the detection of cryptic Structural Variation in patients with intellectual disability and congenital anomaliesFrom1 Oct 2019 → 30 Sep 2023Funding: FWO Applied Biomedical Research (TBM)
- Genetic origin of congenital heart defects in Tunisian population ( a clinical and laboratory approach)From1 Sep 2018 → 2 Sep 2021Funding: Own budget, for example: patrimony, inscription fees, gifts
- DIAGNOSIS AND TREATMENT BY HYDROXYUREA OF CHILDREN WITH SICKLE CELL ANEMIA IN THE DEMOCRATIC REPUBLIC OF CONGO.From1 Jan 2017 → 25 Mar 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- Identification of genetic and genomic causes of syndromic and non-syndromic tooth agenesis (TA).From1 Mar 2016 → 28 Feb 2021Funding: Own budget, for example: patrimony, inscription fees, gifts
- Human genetics in the Democratic Republic of Congo.From1 Oct 2013 → 31 Dec 2015Funding: VLIR-UOS International Conferences (INCO)
Publications
31 - 40 of 426
- DNA testing for sickle cell anemia in Africa: Implementation choices for the Democratic Republic of Congo(2022)
Authors: Gloire Mbayabo, Koenraad Devriendt, Gert Matthijs
- What should we tell parents? Congenital diaphragmatic hernia(2022)
Authors: Francesca Maria Russo, Anne Debeer, Paolo De Coppi, Koenraad Devriendt, Neeltje Crombag, Jan Deprest
Pages: 398 - 407 - Extraocular muscle hypoplasia associated with Axenfeld-Rieger syndrome(2021)
Authors: Catherine Cassiman, Ingele Casteels, Koenraad Devriendt
Pages: 216 - 220 - Two novel presentations of KCNMA1-related pathology--Expanding the clinical phenotype of a rare channelopathy(2021)
Authors: Koenraad Devriendt, Luc De Catte, Marcella Baldewijns
- Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.(2021)
Authors: Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose MG Izarzugaza, Tomas W Fitzgerald, Anne-Karin Kahlert, Alejandro Sifrim, Florian Wünnemann, Yasset Perez-Riverol, Hashim Abdul-Khaliq, et al.
Pages: e1009809 - Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy(2021)
Authors: Koenraad Devriendt, Hilde Van Esch
- Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?(2021)
Authors: Lore Lannoo, Liesbeth Lenaerts, Kris Van Den Bogaert, Huiwen Che, Nathalie Brison, Koenraad Devriendt, Frédéric Amant, Joris Vermeesch, Kristel Van Calsteren
Pages: 1 - 9 - Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease(2021)
Authors: Jeroen Breckpot, Alejandro Sifrim, Koenraad Devriendt, Bernard Thienpont
- Homozygous missense STRADA mutation in a patient with polyhydramnios, megalencephaly and symptomatic epilepsy syndrome(2021)
Authors: Mio Aerden, Liesbeth De Waele, Kris Van Den Bogaert, Koenraad Devriendt
Pages: 121 - 124 - Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations(2021)
Authors: Margot van Riel, Nathalie Brison, Koenraad Devriendt, Lore Lannoo, Kris Van Den Bogaert, Joris Vermeesch
Pages: 1102 - 1108